Schild J A, Mafee M F, Miller M F
Int J Pediatr Otorhinolaryngol. 1984 Jul;7(3):305-10. doi: 10.1016/s0165-5876(84)80013-0.
Wildervanck syndrome is a combination of congenital anomalies characterized by deafness, Klippel-Feil deformity, and an unusual ocular motility disturbance called Duane retraction syndrome. This syndrome is seen infrequently in the general population and may not be recognized since the external appearance of the ears may be normal, and the unusual form of strabismus may not be obvious to the non-ophthalmologist. Patients with the full extent of this triad have a unique appearance. CT examination in these patients delineates the cervical anomalies as well as the inner ear deformity.
怀尔德凡克综合征是一种先天性异常的组合,其特征为耳聋、颈椎融合畸形以及一种称为杜安眼球后退综合征的特殊眼球运动障碍。该综合征在普通人群中很少见,可能未被识别,因为耳朵的外观可能正常,而且这种特殊形式的斜视对于非眼科医生来说可能并不明显。具有这三种全部症状的患者有独特的外貌。对这些患者进行CT检查可清晰显示颈椎异常以及内耳畸形。